Active Ingredient
Alcohol 62% (v/v)
Hand Sanitizing With Lavender Oil Gel
FDA Label NDC 59088-413
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Puretek Corporation for the product Hand Sanitizing With Lavender Oil (NDC 59088-413). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Anti-Bacterial
Uses
■ Hand sanitizer to help reduce bacteria on the skin
Warnings
■ Flammable. Keep away from fire or flame.
When Using This Product
■ do not use in or near eyes. In case of contact, rinse eyes throughly with water
Stop Use And Ask A Doctor If
■ irritation or redness develop and last for more than 72 hours
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
■ Dispense and rub onto hands until dry. Do not rinse off.
■ Children under 6 years of age should use this product under supervision.
■ repeat as necessary
Other Information
■ Do not store above 110°F (43°C)
Inactive Ingredients
Aloe Barbadensis (aloe vera) Leaf Juice, Butyrospermum Parkii (Shea) Butter, Glycerin, Lavandula Angustifolia (Lavender) Oil, Panthenol, Polyacrylate Crosspolymer-6, Water (Aqua)
Genrx Hand Sanitizing Gel With Lavender
Manufactured in the USA by PureTek Corporation
Panorama City, CA 91402 USA
877-921-7873
www.genrxwoundcare.com
List No:41431JLA
NDC 59088-413-08
NDC 59088-413-31
NDC 59088-413-39
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